"DUSP22-related disorder"[Disease/phenotype] AND "PreventionGenetics, - ClinVar - NCBI

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Items: 19

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3051817	NM_001286555.3(DUSP22):c.-5C>T	DUSP22	Single nucleotide variant (5 prime UTR variant +1 more)	DUSP22-related disorder	GLikely benign
Select item 3040278	NM_001286555.3(DUSP22):c.56-6dup	DUSP22	Duplication (intron variant)	DUSP22-related disorder	GLikely benign
Select item 3032831	NM_001286555.3(DUSP22):c.69G>A (p.Ala23=)	DUSP22	Single nucleotide variant (synonymous variant +1 more)	DUSP22-related disorder	GLikely benign
Select item 3052547	NM_001286555.3(DUSP22):c.153G>A (p.Leu51=)	DUSP22	Single nucleotide variant (synonymous variant +1 more)	DUSP22-related disorder	GLikely benign
Select item 3054593	NM_001286555.3(DUSP22):c.168G>A (p.Ala56=)	DUSP22	Single nucleotide variant (synonymous variant +1 more)	DUSP22-related disorder	GLikely benign
Select item 3035996	NM_001286555.3(DUSP22):c.189-4C>T	DUSP22	Single nucleotide variant (intron variant)	DUSP22-related disorder	GLikely benign
Select item 3041169	NM_001286555.3(DUSP22):c.225C>T (p.His75=)	DUSP22	Single nucleotide variant (synonymous variant +1 more)	DUSP22-related disorder	GLikely benign
Select item 3037645	NM_001286555.3(DUSP22):c.285C>T (p.Ser95=)	DUSP22	Single nucleotide variant (synonymous variant +1 more)	DUSP22-related disorder	GLikely benign
Select item 3039993	NM_001286555.3(DUSP22):c.315C>T (p.Thr105=)	DUSP22	Single nucleotide variant (synonymous variant +1 more)	DUSP22-related disorder	GLikely benign
Select item 3035033	NM_001286555.3(DUSP22):c.316G>A (p.Val106Ile)	DUSP22 (V106I)	Single nucleotide variant (missense variant +1 more)	DUSP22-related disorder	GLikely benign
Select item 3049760	NM_001286555.3(DUSP22):c.427G>A (p.Val143Ile)	DUSP22 (V143I)	Single nucleotide variant (missense variant +1 more)	DUSP22-related disorder	GLikely benign
Select item 3039128	NM_001286555.3(DUSP22):c.477G>T (p.Leu159Phe)	DUSP22 (L159F)	Single nucleotide variant (missense variant +1 more)	DUSP22-related disorder	GLikely benign
Select item 3059480	NM_001286555.3(DUSP22):c.573G>A (p.Pro191=)	DUSP22	Single nucleotide variant (synonymous variant +2 more)	DUSP22-related disorder	GBenign
Select item 3042277	NM_001286555.3(DUSP22):c.584C>T (p.Pro195Leu)	DUSP22 (P195L)	Single nucleotide variant (missense variant +2 more)	DUSP22-related disorder	GLikely benign
Select item 3034895	NM_001286555.3(DUSP22):c.594C>T (p.Tyr198=)	DUSP22	Single nucleotide variant (synonymous variant +2 more)	DUSP22-related disorder	GLikely benign
Select item 3032216	NM_001286555.3(DUSP22):c.606G>A (p.Thr202=)	DUSP22	Single nucleotide variant (synonymous variant +2 more)	DUSP22-related disorder	GLikely benign
Select item 3031542	NM_001286555.3(DUSP22):c.*2G>A	DUSP22	Single nucleotide variant (3 prime UTR variant +2 more)	DUSP22-related disorder	GLikely benign
Select item 3057555	NM_001286555.3(DUSP22):c.*8G>A	DUSP22	Single nucleotide variant (3 prime UTR variant +2 more)	DUSP22-related disorder	GLikely benign
Select item 3060833	NM_001286555.3(DUSP22):c.*1878G>A	DUSP22	Single nucleotide variant (3 prime UTR variant +2 more)	DUSP22-related disorder	GBenign